Yamashita Naomi, Tashimo Hiroyuki, Ishida Hirofuni, Matsuo Yukiko, Arai Hidenori, Nagase Hiroyuki, Adachi Tetsuya, Ohta Ken
Department of Pharmacology, Research Institute of Pharmaceutical Sciences, Musashino University, Japan.
Cell Immunol. 2005 Jun;235(2):85-91. doi: 10.1016/j.cellimm.2005.07.006. Epub 2005 Sep 15.
Insulin-like growth factor (IGF)-I is known to act on fibroblasts as a progression factor to push cells toward proliferation and activation to synthesize collagen. Subepithelial fibrosis, collagen deposition at the lamina reticularis, is part of the process of so-called remodeling and is a characteristic finding in the asthmatic airway. To study the role of IGF in the evolution of asthma, we used a model that involved immunization of mice with ovalbumin and alum, followed by an inhaled challenge of ovalbumin. IGF-I neutralizing antibody was continuously infused with an osmotic pump. Pulmonary function was analyzed using whole-body plethysmography before and after acetylcholine administration. It was found that OVA inhalation induced IGF-I expression at the site of the airway. IGF-I neutralizing Ab inhibited the elevation of airway resistance, airway inflammation, and an increase in airway wall thickening. The depression of ICAM-1 expression was accompanied by a diminution in airway inflammation. In conclusion, these results suggest that IGF-I is likely to be an important mediator of inflammation and remodeling in the asthmatic airway.